Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | HCID 140397789 | HCID 140397789 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 86753756 | HCID 86753756 | — |
Reaction Steps
A mixture of 1.05 g of methyl [4-[3-(4-benzyloxycarbonylamidinophenoxy)propyl]-2,3-dioxopiperazin-1-yl]acetate, 0.35 g of 5% palladium-carbon, 0.39 ml of 6N hydrochloric acid and 15 ml of methanol was subjected to hydrogenation at ordinary temperature and atmospheric pressure for 3 hours. Then, the pallasium-carbon was filtered off and the solvent was distilled off under reduced pressure to obtain 0.8 g of methyl [4-[3-(4-amidinophenoxy)propyl]-2,3-dioxopiperazin-1-yl]acetate hydrochloride. The compound obtained was dissolved in 14 ml of 6N hydrochloric acid and the resulting solution was refluxed for 1 hour, after which the solvent was distilled off under reduced pressure to obtain 0.6 g of [4-[3-(4-amidinophenoxy)-propyl]-2,3-dioxopiperazin-1-yl]acetic acid hydrochloride as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06153613 |
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| Source dataset | uspto-grants-2000_11 |
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| ORD ID | ord-b5bbafb3f638409783dd760e683626d6 |
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| Source note | uspto-grants-2000_11 |
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